Multiple system atrophy (MSA) is an adult-onset progressive neurodegenerative disorder that manifests clinically with autonomic failure, parkinsonism, and ataxia in any combination. Oligodendroglial cytoplasmatic inclusions consisting of misfolded α-synuclein are a pathological hallmark of disease. The clinical diagnosis of MSA is typically delayed as a result of incomplete or nonspecific manifestations during ...
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p. 227-230; Submitted by Ana Valéria de Jesus Moura (anavaleria_131@hotmail.com) on 2012-01-03T16:59:26Z No. of bitstreams: 1 10 (1).pdf: 498847 bytes, checksum: a8f8237e5f539a0597be2418e9614285 (MD5); Made available in DSpace on 2012-01-03T16:59:26Z (GMT). No. of bitstreams: 1 10 (1).pdf: 498847 bytes, checksum: a8f8237e5f539a0597be2418e9614285 (MD5) Previous issue date: 1997; The aim of this report was to stu...